Literature DB >> 1551431

Both membrane stretch and fatty acids directly activate large conductance Ca(2+)-activated K+ channels in vascular smooth muscle cells.

M T Kirber1, R W Ordway, L H Clapp, J V Walsh, J J Singer.   

Abstract

Large conductance Ca(2+)-activated K+ channels in rabbit pulmonary artery smooth muscle cells are activated by membrane stretch and by arachidonic acid and other fatty acids. Activation by stretch appears to occur by a direct effect of stretch on the channel itself or a closely associated component. In excised inside-out patches stretch activation was seen under conditions which precluded possible mechanisms involving cytosolic factors, release of Ca2+ from intracellular stores, or stretch induced transmembrane flux of Ca2+ or other ions potentially capable of activating the channel. Fatty acids also directly activate this channel. Like stretch activation, fatty acid activation occurs in excised inside-out patches in the absence of cytosolic constituents. Moreover, the channel is activated by fatty acids which, unlike arachidonic acid, are not substrates for the cyclo-oxygenase or lypoxygenase pathways, indicating that oxygenated metabolites do not mediate the response. Thus, four distinct types of stimuli (cytosolic Ca2+, membrane potential, membrane stretch, and fatty acids) can directly affect the activity of this channel.

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Year:  1992        PMID: 1551431     DOI: 10.1016/0014-5793(92)80319-c

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  45 in total

1.  Voltage-induced membrane displacement in patch pipettes activates mechanosensitive channels.

Authors:  Z Gil; S D Silberberg; K L Magleby
Journal:  Proc Natl Acad Sci U S A       Date:  1999-12-07       Impact factor: 11.205

Review 2.  Large conductance, Ca2+-activated K+ channels (BKCa) and arteriolar myogenic signaling.

Authors:  Michael A Hill; Yan Yang; Srikanth R Ella; Michael J Davis; Andrew P Braun
Journal:  FEBS Lett       Date:  2010-02-20       Impact factor: 4.124

3.  Cell volume and membrane stretch independently control K+ channel activity.

Authors:  Sofia Hammami; Niels J Willumsen; Hervør L Olsen; Francisco J Morera; Ramón Latorre; Dan A Klaerke
Journal:  J Physiol       Date:  2009-03-16       Impact factor: 5.182

4.  Microtubule cytoskeleton involvement in muscarinic suppression of voltage-gated calcium channel current in guinea-pig ileal smooth muscle.

Authors:  T Unno; S Komori; H Ohashi
Journal:  Br J Pharmacol       Date:  1999-08       Impact factor: 8.739

5.  FMRFamide and membrane stretch as activators of the Aplysia S-channel.

Authors:  D H Vandorpe; D L Small; A R Dabrowski; C E Morris
Journal:  Biophys J       Date:  1994-01       Impact factor: 4.033

6.  Functional apical large conductance, Ca2+-activated, and voltage-dependent K+ channels are required for maintenance of airway surface liquid volume.

Authors:  Dahis Manzanares; Carlos Gonzalez; Pedro Ivonnet; Ren-Shiang Chen; Monica Valencia-Gattas; Gregory E Conner; H Peter Larsson; Matthias Salathe
Journal:  J Biol Chem       Date:  2011-03-31       Impact factor: 5.157

7.  Mechanical control of cation channels in the myogenic response.

Authors:  Brian E Carlson; Daniel A Beard
Journal:  Am J Physiol Heart Circ Physiol       Date:  2011-05-13       Impact factor: 4.733

8.  Effect of stretch on calcium channel currents recorded from the antral circular myocytes of guinea-pig stomach.

Authors:  W X Xu; S J Kim; S J Kim; I So; T M Kang; J C Rhee; K W Kim
Journal:  Pflugers Arch       Date:  1996-06       Impact factor: 3.657

9.  Regulation of the electrogenic H+ channel in the plasma membrane of neutrophils: possible role of phospholipase A2, internal and external protons.

Authors:  A Kapus; K Suszták; E Ligeti
Journal:  Biochem J       Date:  1993-06-01       Impact factor: 3.857

10.  Regulatory effect of sulphatides on BKCa channels.

Authors:  S Chi; Z Qi
Journal:  Br J Pharmacol       Date:  2006-10-30       Impact factor: 8.739

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